Interactions between PTEN, TP53, RB1 and TMPRSS2-ERG genes in prostate cancer progression (2021)
- Authors:
- USP affiliated authors: SQUIRE, JEREMY ANDREW - FMRP ; SILVA, FRANCISCO CESAR DE SOUSA E - FMRP
- Unidade: FMRP
- Subjects: NEOPLASIAS PROSTÁTICAS; MUTAÇÃO GENÉTICA; CÉLULAS DENDRÍTICAS; MACRÓFAGOS
- Keywords: Tumor microenvironment; Immune evasion; Immune cell abundance software
- Agências de fomento:
- Language: Inglês
- Imprenta:
- Publisher: Sociedade Brasileira de Genética - SBG
- Publisher place: [Ribeirão Preto]
- Date published: 2021
- Source:
- Título: Resumos
- Conference titles: Congresso Brasileiro de Genética = Brazilian Congress of Genetics
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ABNT
SILVA, Francisco Cesar de Sousa e e MELO, Camila Morais e SQUIRE, Jeremy Andrew. Interactions between PTEN, TP53, RB1 and TMPRSS2-ERG genes in prostate cancer progression. 2021, Anais.. [Ribeirão Preto]: Sociedade Brasileira de Genética - SBG, 2021. Disponível em: https://www.sbg.org.br/anais. Acesso em: 08 out. 2024. -
APA
Silva, F. C. de S. e, Melo, C. M., & Squire, J. A. (2021). Interactions between PTEN, TP53, RB1 and TMPRSS2-ERG genes in prostate cancer progression. In Resumos. [Ribeirão Preto]: Sociedade Brasileira de Genética - SBG. Recuperado de https://www.sbg.org.br/anais -
NLM
Silva FC de S e, Melo CM, Squire JA. Interactions between PTEN, TP53, RB1 and TMPRSS2-ERG genes in prostate cancer progression [Internet]. Resumos. 2021 ;[citado 2024 out. 08 ] Available from: https://www.sbg.org.br/anais -
Vancouver
Silva FC de S e, Melo CM, Squire JA. Interactions between PTEN, TP53, RB1 and TMPRSS2-ERG genes in prostate cancer progression [Internet]. Resumos. 2021 ;[citado 2024 out. 08 ] Available from: https://www.sbg.org.br/anais - Differential gene expression related to TMPRSS2-ERG fusion, CDK12, RB1, TP53, AR and ZEB1 based on transcriptomic analysis of the TCGA PRAD cohort
- Frequência de TP53 na modulação do microambiente tumoral e progressão do câncer da próstata
- Analysis of the impact of ZEB1 expression on pathway enrichment and immune cell abundance in prostate cancer
- Quantitative assessment of PTEN loss (qPTEN) is strongly associated with biochemical recurrence and may improve treatment decisions after surgery
- Tumour genomic and microenvironmental heterogeneity for integrated prediction of 5-year biochemical recurrence of prostate cancer: a retrospective cohort study
- Digital expression profiling identifies RUNX2, CDC5L, MDM2, RECQL4, and CDK4 as potential predictive biomarkers for neo-adjuvant chemotherapy response in paediatric osteosarcoma
- Recurrent copy number alterations in prostate cancer: an in silico meta-analysis of publicly available genomic data
- Extracellular vesicles: evolving factors in stem cell biology
- The Terry Fox Research Institute Canadian Prostate Cancer Biomarker Network: an analysis of a pan-Canadian multi-center cohort for biomarker validation
- In silico shows that PTEN loss and AR overexpression are associated with increased CD8+ T-cell and Treg density and earlier disease recurrence in prostate cancer
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